产品名称
Flucloxacillin sodium, ≥95% (HPLC)
SMILES string
[Na+].Fc1c(c(ccc1)Cl)c2n[o]c(c2\C(=N\[C@H]3[C@H]4SC([C@@H](N4C3=O)C(=O)O)(C)C)\[O-])C
InChI key
OTEANHMVDHZOPB-SLINCCQESA-M
InChI
1S/C19H17ClFN3O5S.Na/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24;/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28);/q;+1/p-1/t13-,14+,17-;/m1./s1
assay
≥95% (HPLC)
form
powder
storage condition
protect from light
color
white to beige
storage temp.
−20°C
Quality Level
General description
Flucloxacillin sodium, a sodium salt of flucloxacillin, is a member of the penicillin class.
Application
Flucloxacillin sodium has been used as a β-lactam antibiotic to study its effects on methicillin-resistant Staphylococcus aureus (MRSA) ΔfloA mutant.
Biochem/physiol Actions
Flucloxacillin is a narrow-spectrum β-lactam antibiotic used to treat Gram-positive bacterial infections. Flucloxacillin induces cholestatic liver damage.
Flucloxacillin is a narrow-spectrum β-lactam antibiotic.
Flucloxacillin exhibits antimicrobial property.
Other Notes
Light sensitive
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Handbook of Pharmaceutical Excipients (2014)
Apparent Molar Volume, Adiabatic Compressibility, and Critical Micelle Concentration of Flucloxacillin Sodium in Aqueous NaCl Solutions at Different Temperatures
Khatun MR, et al.
Journal of Chemical and Engineering Data, 61(1), 102-113 (2016)
Membrane microdomain disassembly inhibits MRSA antibiotic resistance
Garcaa-Fernandez E, et al.
Cell, 171(6), 1354-1367 (2017)
Esther García-Fernández et al.
Cell, 171(6), 1354-1367 (2017-11-07)
A number of bacterial cell processes are confined functional membrane microdomains (FMMs), structurally and functionally similar to lipid rafts of eukaryotic cells. How bacteria organize these intricate platforms and what their biological significance is remain important questions. Using the pathogen
Ryan Nattrass et al.
Toxicological sciences : an official journal of the Society of Toxicology, 146(1), 146-156 (2015-04-17)
There are currently no animal models of drug-induced liver injury (DILI) where the adaptive immune system has been shown to damage the liver. Thus, it is difficult to explore the mechanistic basis of the tissue injury. The aim of this
商品
Bioactive small molecules for immune system signaling target identification/validation and antibiotics, antivirals, and antifungals offered.
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